Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 198791018 | Methionine adenosyltransferase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 796501013 | Hepatic methionine adenosyltransferase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 96167011 | Hepatic methionine adenosyltransferase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 96168018 | MAT deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hepatic methionine adenosyltransferase deficiency (disorder) | morphologie associée (attribut) | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | localisation d'une constatation (attribut) | système digestif | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Digestive system hereditary disorder | false | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Enzymopathy | true | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Congenital anomaly of liver | false | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Hypermethioninaemia | true | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Inborn error of metabolism | true | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Congenital anomaly of abdomen | false | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | est un(e) (attribut) | Congenital anomaly of body cavity | false | Inferred relationship | Some | ||
| Hepatic methionine adenosyltransferase deficiency (disorder) | localisation d'une constatation (attribut) | foie | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | morphologie associée (attribut) | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | localisation d'une constatation (attribut) | foie | false | Inferred relationship | Some | 1 | |
| Hepatic methionine adenosyltransferase deficiency (disorder) | localisation d'une constatation (attribut) | organe digestif (structure corporelle) | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR